2-Amino-6-methyl-3-nitropyridine

98%

Reagent Code: #134587
label
Alias 2-amino-3-nitro-6-methylpyridine
fingerprint
CAS Number 21901-29-1

science Other reagents with same CAS 21901-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₆H₇N₃O₂
badge Registry Numbers
MDL Number MFCD00047443
thermostat Physical Properties
Melting Point 147-157 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. It serves as a building block for more complex nitrogen-containing heterocyclic compounds. Its nitro and amino functional groups allow for further chemical modifications, enabling its use in dye manufacturing and in the development of specialty chemicals. Commonly employed in research settings for designing novel bioactive molecules due to its pyridine backbone, which is prevalent in many biologically active compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿159.50
5g
10-20 days ฿275.00
25g
10-20 days ฿1,540.00
100g
10-20 days ฿6,140.00
500g
10-20 days ฿30,470.00
2-Amino-6-methyl-3-nitropyridine
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. It serves as a building block for more complex nitrogen-containing heterocyclic compounds. Its nitro and amino functional groups allow for further chemical modifications, enabling its use in dye manufacturing and in the development of specialty chemicals. Commonly employed in research settings for designing novel bioactive molecules due to its pyridine b

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. It serves as a building block for more complex nitrogen-containing heterocyclic compounds. Its nitro and amino functional groups allow for further chemical modifications, enabling its use in dye manufacturing and in the development of specialty chemicals. Commonly employed in research settings for designing novel bioactive molecules due to its pyridine backbone, which is prevalent in many biologically active compounds.

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